Access to Care and Health-Related Quality of Life in Multiple Sclerosis

被引:0
|
作者
Marrie, Ruth Ann [1 ,2 ]
Lancia, Samantha [3 ]
Cutter, Gary R. [4 ]
Fox, Robert J. [5 ]
Salter, Amber [3 ]
机构
[1] Univ Manitoba, Dept Internal Med, Winnipeg, MB, Canada
[2] Univ Manitoba, Max Rady Coll Med, Rady Fac Hlth Sci, Dept Community Hlth Sci, Winnipeg, MB, Canada
[3] UT Southwestern, Dept Neurol, Sect Stat Planning & Anal, Dallas, TX USA
[4] Univ Alabama Birmingham, Dept Biostat, Birmingham, AB, Canada
[5] Cleveland Clin, Neurol Inst, Mellen Ctr Multiple Sclerosis, Cleveland, OH USA
关键词
D O I
10.1212/CPJ.0000000000200338
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and ObjectivesDespite their high health care use, it is unclear whether the health care needs of people with MS are being met and what their priorities are. We assessed priorities for access to, and affordability of care, by people living with MS in the United States. We also tested the association between perceived inadequate access to care and health-related quality of life (HRQoL).MethodsIn Fall 2022, we conducted a cross-sectional survey of participants in the North American Research Committee on Multiple Sclerosis Registry about access to care and HRQoL (Health Utilities Index Mark III). We used multivariable polytomous logistic regression to test sociodemographic and clinical factors associated with access to care. We used multivariable linear regression analysis to test the association between access to care and HRQoL.ResultsWe included 4,914 respondents in the analysis, of whom 3,974 (80.9%) were women, with a mean (SD) age 64.4 (9.9) years. The providers who were most reported as needed but inaccessible were complementary providers (35.5%), followed by allied health providers (24.2%), occupational therapists (22.7%), and mental health providers (20.7%). Over 80% of participants reported that it was important or very important to be able to get an appointment with their primary MS health care provider when needed, to have sufficient time in their appointments to explain their concerns, to see their neurologist if their status changed, and that their health care providers communicated to coordinate their care. Participants who reported needing to see the provider but not having access or seeing the provider but would like to see them more often had lower HRQOL (ranging from -0.059 to -0.176) than participants who saw the provider as much as needed.DiscussionGaps in access to care persist for people with MS in the United States and substantially affect HRQoL. Improving access to care for people with MS should be a health system priority.
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页数:13
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